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Effect of Stress Management Program on Psychological Distress of Cancer Patients and Caring Burden and Quality of Life of Their Caregivers

Effect of Stress Management Program on Psychological Distress of Cancer Patients and Caring Burden and Quality of Life of Their Caregivers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180728040617N3
Enrollment
60
Registered
2021-03-14
Start date
2024-01-16
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer. Malignant neoplasms

Interventions

Intervention 1: Intervention group: For the intervention group, 4 weekly sessions of 60 minutes are held in the form of participation in a group video call (webinar) in the form of lectures, group dis

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: Caregiver and patient age at least 15 years. No psychological disorders in the caregiver. No drug addiction in the caregiver. No hearing or vision impairment in the caregiver. The caregiver should have the most contact with the patient. Ability to access the Internet and online mass communication software. Have the minimum ability to use smartphones and social networks. Non-participation in other supportive interventions. The caregiver should not be a member of the health care system. The caregiver is a family member of the patient. The definitive diagnosis of cancer has been made by a doctor. The stage of the disease of each patient is known Patients undergo chemotherapy.

Exclusion criteria

Exclusion criteria: Do not participate in the post-test. Absence from more than two sessions in support sessions. The reluctance of the caregiver to participate in the sessions. Patient death during the study Transfer the patient to other medical centers Occurrence of stressful events (except for the usual treatment process) for the patient or caregiver

Design outcomes

Primary

MeasureTime frame
Caregivers Caring burden. Timepoint: At the beginning of the study (before the intervention) and 7 days after intervention. Method of measurement: Novak & Guest Caring Burden Questionnaire.;Caregivers Quality of Life. Timepoint: At the beginning of the study (before the intervention) and 7 days after intervention. Method of measurement: Quality of Life Questionnaire SF-36.

Secondary

MeasureTime frame
Patients' psychological distress. Timepoint: At the beginning of the study (before the intervention) and 7 days after intervention. Method of measurement: Lovibond Depression, Anxiety and Stress Scale (DASS-21).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedmohammad Mirhosseini

Shahroud University of Medical Sciences

mirhoseinim@shmu.ac.ir+98 23 3239 3811

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026